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1.
Acta Physiol Pharmacol Latinoam ; 34(2): 157-62, 1984.
Artigo em Inglês | MEDLINE | ID: mdl-6240915

RESUMO

When mice fed on a protein-depleted diet are restored to the normal diet (re-feeding), there is a 2-fold increase in liver RNA polymerase I activity. The results obtained with pactamycin; an inhibitor of protein synthesis, suggest the presence of short-lived proteins which are required for inducing an activated state of transcription. To gain an insight on whether ornithine decarboxylase (ODC)--the first enzyme in polyamine biosynthesis--is the labile protein that regulates rRNA synthesis, we have investigated the correlation between liver ODC and RNA polymerase I activities under different nutritional conditions. We have also studied the effects of alpha-difluormethylornithine (alpha-DFMO)--a specific ODC inactivator--on rRNA transcription. The results indicate that, after re-feeding, there is an abrupt increase in ODC activity that rapidly declines, while RNA polymerase I is still increasing. On the other hand, alpha-DFMO--which inhibits the elevated activity of ODC--has not effect on rRNA transcription.


Assuntos
Dieta , Fígado/enzimologia , Ornitina Descarboxilase/metabolismo , RNA Polimerase I/metabolismo , Animais , Eflornitina , Masculino , Camundongos , Camundongos Endogâmicos , Ornitina/análogos & derivados , Ornitina/metabolismo , Inibidores da Ornitina Descarboxilase , Deficiência de Proteína/metabolismo
2.
Artigo em Inglês | BINACIS | ID: bin-49665

RESUMO

When mice fed on a protein-depleted diet are restored to the normal diet (re-feeding), there is a 2-fold increase in liver RNA polymerase I activity. The results obtained with pactamycin; an inhibitor of protein synthesis, suggest the presence of short-lived proteins which are required for inducing an activated state of transcription. To gain an insight on whether ornithine decarboxylase (ODC)--the first enzyme in polyamine biosynthesis--is the labile protein that regulates rRNA synthesis, we have investigated the correlation between liver ODC and RNA polymerase I activities under different nutritional conditions. We have also studied the effects of alpha-difluormethylornithine (alpha-DFMO)--a specific ODC inactivator--on rRNA transcription. The results indicate that, after re-feeding, there is an abrupt increase in ODC activity that rapidly declines, while RNA polymerase I is still increasing. On the other hand, alpha-DFMO--which inhibits the elevated activity of ODC--has not effect on rRNA transcription.

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